510(k) K925159 ยท KOI Stimulator, Nerve, Peripheral, Electric
TOF-GUARD TRANSMISSION MONITOR
| Applicant | Biometer Intl. A/S, Denmark, DK |
| Decision | Substantially Equivalent, Sep 1, 1993 |
| Received | Oct 13, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925159
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.